Recruiting
Phase 1

RGT-419B with Endocrine Therapy

Sponsor:

Regor Pharmaceuticals Inc.

Code:

NCT05304962

Conditions

Breast Cancer

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

RGT-419B

RGT-419B in combination with hormonal therapy

Study Details

Brief summary:

This is a phase I, First-in-Human (FIH), open-label study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, and preliminary efficacy of RGT-419B administered orally as monotherapy OR in combination with Hormonal Therapy in subjects with HR+, HER2- locally advanced and unresectable (Stage III) or metastatic (Stage IV) breast cancer whose disease has progressed during prior therapy with an approved CDK4/6i plus hormonal therapy.

Conditions

Breast Cancer

Study ID

NCT05304962

Start date

Mar 4, 2022

Status verified date

Aug, 2026

Completion date

Mar 31, 2027

Anticipated

Primary completion date

Dec 30, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Male or female >/= 18 years old
2. ECOG Performance Status 0 to 1
3. Subjects must have histologically or cytologically confirmed diagnosis of ER+, HER2- ABC consistent with ASCO CAP guidelines that is locally advanced and unresectable (Stage III) or metastatic (Stage IV) BC.
4. Measurable AND evaluable lesions at baseline per RECIST v1.1.
5. Eligible subjects must meet all of the following criteria:

  • Progression after receiving 1 line of prior cyclin-dependent kinase 4 and 6 inhibitor (CDK4/6i) therapy combined with HT in the MBC setting (up to 1 additional line of CDK4/6i is permitted in the post-surgical adjuvant setting);

  • Subjects must have received therapy for ≥3 months in the MBC setting, or for ≥6 months in the adjuvant setting, prior to progression
  • Progression after ≤3 lines of prior HT therapy (regardless of whether it is HT alone or in combination with other therapies)

  • Prior HT combination agents, including SERD, SERM or AI, must have received formal approval by regulatory agency.
  • ≤ 1 prior line of chemotherapy in the metastatic setting
6. Adequate organ function
7. Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

1. Presence of visceral metastases with severe organ dysfunction as evidence by signs and symptoms, laboratory studies, lymphangitic spread and/or rapid progression of disease
2. Pregnant or planning to become pregnant
3. Prior irradiation to >25% of the bone marrow and/or inadequate bone marrow function or evidence of clinically significant end-organ damage
4. Major surgery, chemotherapy, targeted therapy, experimental agents, or radiation within 14-28 days prior to Cycle 1, Day 1
5. Active, serious medical condition that is not well controlled with locally approved medications allowed by the protocol
6. History of allergic reactions attributed to compounds of similar chemical or biologic composition to the drugs used in the study

Study Design

Enrollment

64 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Arm A

RGT-419B given alone as monotherapy

experimental: Arm B

RGT-419B in combination with Hormonal Therapy

Interventions

RGT-419B

oral capsules

RGT-419B in combination with hormonal therapy

RGT-419B in combination with hormonal therapy (Selective Estrogen Receptor Degrader, Selective Estrogen Receptor Modulator, or Aromatase Inhibitor)

Primary outcome measure

  • Safety & Tolerability - Number of subjects with Dose-Limiting Toxicities (DLTs) at each cohort dose level in singlet and doublet therapy [ Time Frame: 4 weeks (1 cycle) ]

Central Contacts and Locations

Central contacts

Regor Pharmaceuticals Central Office

617-315-9070rgt-419b_01-101@regor.com

Locations

University of California, San Diego

Recruiting

La Jolla, California, United States, 92037

Contacts

Principal Investigator:

Rebecca Shatsky, MD

University California, Los Angeles

Recruiting

Los Angeles, California, United States, 90404

Contacts

Principal Investigator:

Saeed Sadeghi, MD

Moffitt Cancer Center

Recruiting

Tampa, Florida, United States, 33612

Contacts

Principal Investigator:

Heather Han, MD

Emory University

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

Principal Investigator:

Kevin Kalinsky, MD, MS

Massachusetts General Hospital

Recruiting

Boston, Massachusetts, United States, 02142

Contacts

Principal Investigator:

Seth Wander, MD

Washington University School of Medicine

Recruiting

St Louis, Missouri, United States, 63110

Contacts

Principal Investigator:

Katherine Clifton, MD

New York Cancer and Blood Specialists

Recruiting

Port Jefferson Station, New York, United States, 11776

Contacts

Principal Investigator:

Richard Zuniga, MD

More Information

Sponsor

Regor Pharmaceuticals Inc.

Last update posted

Aug 12, 2026

Last verified

Aug, 2026

Keywords

  • Breast Cancer

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Regor Pharmaceuticals Inc. on 2026-08-12.